Allele Registry

Canonical Allele Identifier: PA2826635363

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000697376

RCV001756216

RCV003999664

ClinVar Variation:

575217

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Leu315Phe	CA346749707 NM_001281494.2:c.943C>T